Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270820Generated: November 1, 2026

Acetic Acid → HCID 178525127, compound

https://huagongshe.com/reaction/1270820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantO-XyleneHCID 7237—
ReactantAmmonium AcetateHCID 517165—
Reactant2-(2-Oxo-2-phenyl-ethylcarbamoyl)-piperidine-1-carboxylic acid benzyl esterHCID 23570718—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178525127HCID 178525127—

Reaction Conditions

Temperature165 °C

Reaction Steps

2-(2-Oxo-2-phenyl-ethylcarbamoyl)-piperidine-1-carboxylic acid benzyl ester (22.83 g, 60 mmol), NH4OAc (ammonium acetate) (63.5 g, 824 mmol), AcOH (acetic acid) (30 mL), and xylene (350 mL) were mixed at room temperature, and with stirring the reaction mixture was warmed in an oil bath at 165° C. for about 6 hours. The reaction mixture was then cooled to room temperature and poured into brine. The organic phase was dried over MgSO4, filtered, and concentrated under reduced pressure to yield 31.24 g of off white powder. This sample was triturated in ethyl ether (100 mL), filtered, and rinsed liberally with ethyl ether to yield 15.12 g (70% over two steps) of the desired product 2-(4-phenyl-1H-imidazol-2-yl)-piperidine-1-carboxylic acid benzyl ester as a white solid. HPLC analysis showed the compound to be 100% pure at 254 nm and 98.1% pure at 214 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202381B2
Source datasetuspto-grants-2007_04
ORD IDord-2f06edc357b344899a99cce581a9d35b
Source noteuspto-grants-2007_04